Canonical Allele Identifier: CA714361097
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1459601635
gnomAD v3: 15-58749949-C-T
gnomAD v4: 15-58749949-C-T
MyVariant Identifiers: chr15:g.59042148C>T (hg19) chr15:g.58749949C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749949C>T , CM000677.2:g.58749949C>T GRCh38
NC_000015.9:g.59042148C>T , CM000677.1:g.59042148C>T GRCh37
NC_000015.8:g.56829440C>T NCBI36
NG_033876.1:g.5030G>A
NG_033876.2:g.4759G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-415G>A ENSP00000260408.3:n.-415G>A
NM_001110.3:c.-415G>A NP_001101.1:n.-415G>A
NM_001320570.1:c.-415G>A NP_001307499.1:n.-415G>A
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